ВОзвращает список болезней. Можно фильтр/искать

search, age, gender, parent, symptoms, sort_name, sort_by, rand, branches
GET /disease/?format=api&ordering=-who&page=424
HTTP 200 OK
Allow: GET, HEAD, OPTIONS
Content-Type: application/json
Vary: Accept

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            },
            "code": "C26.1",
            "name": "Рак селезенки",
            "icd_name": "Рак селезенки",
            "gender": 0,
            "age_min": 40,
            "age_max": 100,
            "cause": [
                "0"
            ],
            "periodicity": 1,
            "slug": "c26.1_rak_selezenki",
            "lead": "очаговые разрастания морфологически измененной опухолевой ткани в селезеночной паренхиме",
            "description": "",
            "etiology": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Причины первичной опухолевой трансформации тканей селезенки окончательно не установлены. При вторичных новообразованиях процесс провоцируется системным поражением лимфоидной ткани или метастатическим распространением клеток. Точных доказательств, подтверждающих наследственный характер неоплазии, нет. По мнению специалистов, возможными этиологическими факторами первичных и вторичных селезеночных новообразований являются:</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Воздействие повреждающих факторов. Патологическое разрастание тканей селезенки может происходить под воздействием ионизирующего излучения, инфекционных агентов, вирусов с онкогенным действием. Помимо этого, развитие неоплазии иногда связывают с влиянием полиароматических углеводородов и никотина, обладающих канцерогенным потенциалом. Иногда заболевание возникает на фоне ишемии или прямого повреждения паренхимы селезенки при травмах, а также вследствие паразитарного поражения органа.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Наличие внеселезеночных опухолей. Вторичное опухолевое изменение характерно для злокачественных лимфопролиферативных процессов &mdash; лимфогранулематоза, ретикулосарком, лимфолейкоза. В некоторых случаях поражение селезенки является единственным проявлением этих онкологических заболеваний. Метастазы в селезенку наблюдаются редко.</span></p>",
            "pathogenesis": "<p>&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Основой механизма развития первичных и лимфопролиферативных опухолей селезенки являются неопластическая конверсия клеток и онкогенез. Под действием мутагенных факторов повреждается клеточная ДНК, ткани изменяют антигенный состав, в большей или меньшей мере утрачивают органоспецифическую структуру и функциональность. Из-за нарушения механизмов, контролирующих деление, рост, запрограммированную гибель (апоптоз) клетки селезенки начинают бесконтрольно делиться, формируя узлы патологической ткани. Растущая в объеме опухоль сдавливает, а при злокачественном процессе и прорастает окружающую паренхиму, капсулу, сосудисто-нервную ножку, смежные органы. При метастатическом механизме образования лиенальных неоплазий в формировании структуры патологических очагов участвуют анормальные клетки основного новообразования.</span></p>",
            "diagnostics": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">План обследования пациента с подозрением на опухоль селезенки включает следующие инструментальные и лабораторные методы:</span></p>\r\n<ul>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">УЗИ селезенки. При проведении ультразвукового исследования визуализируют структуру паренхимы, оценивают размеры и топографию органа. Иногда дополнительно назначают УЗДГ селезенки, по результатам которого можно судить о кровоснабжении подозрительных узлов, скорости кровотока в селезеночных артериях, венах.</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">КТ брюшной полости. Рентгенологическое исследование с болюсным внутривенным введением контрастного препарата помогает отграничить неизмененную паренхиму от некротических очагов, которые не накапливают контраст. Компьютерная томография имеет высокую информативность и обеспечивает обнаружение опухолей в 95% случаев.</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Целиакография. Катетеризация чревного ствола, введение контраста с выполнением серии рентгенологических снимков позволяет оценить состояние артерий абдоминальных органов. При наличии опухолей на рентгенограмме обнаруживают бессосудистый участок или новообразованные сосуды в области проекции селезенки, выраженное смещение крупных артерий и вен.</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Гистологический анализ. Морфологическое исследование пунктата селезенки назначается для уточнения характера процесса, проведения дифференциальной диагностики между доброкачественными и злокачественными новообразованиями. Основными признаками опухолевого поражения являются наличие атипичных клеток с патологическими митозами, потеря дифференцировки.</span></li>\r\n</ul>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p>&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">В клиническом анализе крови выявляется значительное повышение СОЭ (более 20 мм/ч), резкое снижение количества эритроцитов и гемоглобина. Иногда наблюдается увеличение процентного содержания нейтрофилов. В биохимическом анализе крови определяется уменьшение количества общего белка за счет альбуминов, повышение показателей мочевины. При оценке результатов коагулограммы обнаруживается повышение свертывающей способности крови со склонностью к тромбозам. При затруднениях в постановке диагноза может выполняться МРТ органов брюшной полости.</span></p>",
            "treatment": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Если нет серьезных противопоказаний к проведению операции, то опухоль селезенки удаляется посредством хирургического вмешательства. При выборе хирургической тактики учитывают морфологическое строение неоплазии, ее размеры, расположение, взаимоотношение с окружающими органами.&nbsp;</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 7pt; font-family: Verdana; background-color: transparent; font-style: normal; font-variant-numeric: normal; font-variant-east-asian: normal; vertical-align: baseline; white-space: pre-wrap;\">Если опухоль селезенки имеет вторичный характер и возникла на фоне какого-либо онкологического процесса в других органах и тканях также потребуется проведение терапии основного заболевания. Объем операции и метод хирургического вмешательства зависит от размеров, расположения (центральная, периферическая), от тяжести состояния пациента по сопутствующей терапевтической патологии. Для лечения опухолей выполняют резекцию органа, спленэктомию, при злокачественных поражениях в послеоперационном периоде проводят химиотерапию.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Рекомендованными видами вмешательств являются:</span></p>\r\n<ul>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Резекция селезенки. Органосохраняющие операции производят только для удаления небольших доброкачественных опухолей.</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Спленэктомия. Удаление селезенки необходимо при массивных доброкачественных неоплазиях, поразивших большую часть пульпы, злокачественных процессах. Предпочтителен менее травматичный лапароскопический метод операции. Пациентам со злокачественными образованиями после операции назначают химиотерапию.</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Лечение опухолей, возникших в рамках лимфопролиферативных процессов или метастатического поражения селезенки, производится по соответствующим медицинским протоколам и предполагает назначение лучевой, таргетной, химиотерапии.</span></li>\r\n<li><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Вопрос об удалении селезенки в каждом случае решается индивидуально, у некоторых пациентов спленэктомия оказывает положительный эффект на течение основного заболевания.</span></li>\r\n</ul>\r\n<p>&nbsp;</p>\r\n<p><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">&nbsp;</span></p>",
            "prevention": "<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">Способы специфической профилактики пока не разработаны, однако при появлении первых симптомов следует обратиться к специалисту. При доброкачественных процессах удаление опухоли обычно позволяет добиться полного излечения пациента. Своевременная диагностика и адекватное комбинированное лечение злокачественных новообразований селезенки на ранних стадиях существенно увеличивает благоприятный прогноз и шансы на выздоровление.</span></p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\">&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">В ходе некоторых исследований была обнаружена связь между хроническим гепатитом C и B-клеточной неходжкинской лимфомой. Принятие мер по предотвращению гепатита С может помочь пациентам снизить риск этого заболевания.</span></p>\r\n<p>&nbsp;</p>",
            "clinical_picture": "<p>&nbsp;</p>\r\n<p style=\"line-height: 1.38; margin-top: 0pt; margin-bottom: 0pt;\" dir=\"ltr\"><span style=\"font-size: 6.999999999999999pt; font-family: Verdana; color: #000000; background-color: transparent; font-weight: 400; font-style: normal; font-variant: normal; text-decoration: none; vertical-align: baseline; white-space: pre-wrap;\">При малых размерах опухолей заболевание длительное время протекает бессимптомно с минимальной выраженностью клинических проявлений. У пациента наблюдается синдром &laquo;малых признаков&raquo;: утомляемость, слабость, ухудшение работоспособности, потеря аппетита, депрессия, снижение массы тела. По мере прогрессирования опухоли (вплоть до разрыва селезенки) пациента начинают беспокоить боли постоянного характера, возникает тяжесть в области левого подреберья, чувство распирания, асимметрия и увеличение живота, длительная субфебрильная температура, болезненные ощущения в левых отделах брюшной полости. Иногда боль иррадиирует в левое надплечье и плечо. При значительном увеличении размеров селезенки и вовлечении в процесс соседних органов могут наблюдаться расстройства мочеиспускания, не поддающаяся медикаментозной терапии артериальная гипертензия, отеки нижних конечностей.</span></p>",
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            },
            "code": "C92",
            "name": "Миелоидный лейкоз",
            "icd_name": "Миелоидный лейкоз [миелолейкоз]",
            "gender": 0,
            "age_min": 1,
            "age_max": 100,
            "cause": [
                3,
                0
            ],
            "periodicity": 4,
            "slug": "c92_mieloidnyy_leykoz",
            "lead": " это злокачественная опухоль миелоидного ростка крови, при которой быстро размножаются изменённые белые кровяные клетки. ",
            "description": "Миелоидный лейкоз (МЛ) – это раковое заболевание крови, которое характеризуется большим содержанием аномальных незрелых лейкоцитов, размножающихся очень быстро. Этот тип лейкоза поражает 20% детей с раковыми заболеваниями крови. ",
            "etiology": "<p>Точные причины возникновения  миелоидного лейкоза неизвестны, но онкологи выделяют некоторые условия, которые способствуют повышению риска заболевания.</p>\r\n<p>Риски включают в себя унаследованные генетические проблемы, такие, как синдром Дауна, нейрофиброматоз, а также анемия Фанкони и прочие наследуемые патологии костного мозга. Ненаследуемые заболевания – миелодиспластический синдром и апластическая анемия, также могут увеличить риск развития острой лейкемии.МЛ чаще встречается у детей, которые были подвержены лучевой или химиотерапии, и является наиболее распространенным типом вторичного рака у детей.</p>\r\n<p>Если у одного из близнецов диагностировали лейкемию в возрасте до 6 лет, то вероятность развития миелоидного лейкоза у второго ребенка составляет 20-25%. Дети, имеющие сестер и братьев с лейкемией, заболевают в два раза чаще. Облучение во время беременности может вызвать заболевание у развивающегося плода. Некоторые экологические факторы также могут провоцировать лейкоз.</p>",
            "pathogenesis": "",
            "diagnostics": "<p>Полный анализ крови, назначающийся при первых признаках рака крови, дает врачу важную информацию о количестве нормальных клеток крови в организме, а также о том, насколько хорошо функционируют печень, селезенка и другие органы.</p>\r\n<p>Аспирация и биопсия необходимы для изучения костного мозга. Врач вводит иглу в большую кость, как правило, бедренную, и берет небольшое количество костного мозга для проверки его на наличие раковых клеток.</p>\r\n<p>Рентген, МРТ и УЗИ помогают обнаружить увеличение органов и исключить симптомы других заболеваний.</p>\r\n<p>Спинномозговая пункция – процедура для диагностики рака крови, при которой берется немного спинномозговой жидкости для исследования в лаборатории.</p>\r\n<p>Для идентификации подтипов МЛ проводятся хромосомные тесты. При этом для анализа ДНК берутся клетки крови и костного мозга.</p>",
            "treatment": "<p>Миелоидный лейкоз прогрессирует быстро, поэтому своевременная диагностика играет особенно важную роль. Онкологи не выделяют промежуточных стадий МЛ, а характеризуют заболевание либо как вновь диагностированное, либо как находящееся в стадии ремиссии. Ремиссия – состояние, при котором нет никаких признаков присутствия болезни в организме.</p>\r\n<p>Лечение состоит из двух этапов. Первый этап, или фаза индукции, преследует цель убить как можно большее количество раковых клеток в организме и достигнуть состояния ремиссии. Второй этап, или фаза пост-ремиссии, предназначен для поддержания эффекта терапии и преодоления последствий лечения. I и II этапы могут включать несколько видов терапии, использующихся независимо или совместно друг с другом.</p>\r\n<p>Химиотерапия – это уничтожение раковых клеток специальными препаратами. Интерканальная терапия осуществляется через поясничный прокол и обеспечивает поступление лекарства непосредственно в спинномозговую жидкость, где может скапливаться большое количество пораженных лейкоцитов.</p>\r\n<p>В случае необходимости, после химиотерапии проводится трансплантация костного мозга. Новые здоровые стволовые клетки нужны для восстановления нормального состояния иммунной системы и крови.</p>",
            "prevention": "",
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            },
            "code": "C92",
            "name": "Миелоидный лейкоз",
            "icd_name": "Миелоидный лейкоз [миелолейкоз]",
            "gender": 0,
            "age_min": 1,
            "age_max": 100,
            "cause": [
                3,
                0
            ],
            "periodicity": 4,
            "slug": "c92_mieloidnyy_leykoz",
            "lead": " это злокачественная опухоль миелоидного ростка крови, при которой быстро размножаются изменённые белые кровяные клетки. ",
            "description": "Миелоидный лейкоз (МЛ) – это раковое заболевание крови, которое характеризуется большим содержанием аномальных незрелых лейкоцитов, размножающихся очень быстро. Этот тип лейкоза поражает 20% детей с раковыми заболеваниями крови. ",
            "etiology": "<p>Точные причины возникновения  миелоидного лейкоза неизвестны, но онкологи выделяют некоторые условия, которые способствуют повышению риска заболевания.</p>\r\n<p>Риски включают в себя унаследованные генетические проблемы, такие, как синдром Дауна, нейрофиброматоз, а также анемия Фанкони и прочие наследуемые патологии костного мозга. Ненаследуемые заболевания – миелодиспластический синдром и апластическая анемия, также могут увеличить риск развития острой лейкемии.МЛ чаще встречается у детей, которые были подвержены лучевой или химиотерапии, и является наиболее распространенным типом вторичного рака у детей.</p>\r\n<p>Если у одного из близнецов диагностировали лейкемию в возрасте до 6 лет, то вероятность развития миелоидного лейкоза у второго ребенка составляет 20-25%. Дети, имеющие сестер и братьев с лейкемией, заболевают в два раза чаще. Облучение во время беременности может вызвать заболевание у развивающегося плода. Некоторые экологические факторы также могут провоцировать лейкоз.</p>",
            "pathogenesis": "",
            "diagnostics": "<p>Полный анализ крови, назначающийся при первых признаках рака крови, дает врачу важную информацию о количестве нормальных клеток крови в организме, а также о том, насколько хорошо функционируют печень, селезенка и другие органы.</p>\r\n<p>Аспирация и биопсия необходимы для изучения костного мозга. Врач вводит иглу в большую кость, как правило, бедренную, и берет небольшое количество костного мозга для проверки его на наличие раковых клеток.</p>\r\n<p>Рентген, МРТ и УЗИ помогают обнаружить увеличение органов и исключить симптомы других заболеваний.</p>\r\n<p>Спинномозговая пункция – процедура для диагностики рака крови, при которой берется немного спинномозговой жидкости для исследования в лаборатории.</p>\r\n<p>Для идентификации подтипов МЛ проводятся хромосомные тесты. При этом для анализа ДНК берутся клетки крови и костного мозга.</p>",
            "treatment": "<p>Миелоидный лейкоз прогрессирует быстро, поэтому своевременная диагностика играет особенно важную роль. Онкологи не выделяют промежуточных стадий МЛ, а характеризуют заболевание либо как вновь диагностированное, либо как находящееся в стадии ремиссии. Ремиссия – состояние, при котором нет никаких признаков присутствия болезни в организме.</p>\r\n<p>Лечение состоит из двух этапов. Первый этап, или фаза индукции, преследует цель убить как можно большее количество раковых клеток в организме и достигнуть состояния ремиссии. Второй этап, или фаза пост-ремиссии, предназначен для поддержания эффекта терапии и преодоления последствий лечения. I и II этапы могут включать несколько видов терапии, использующихся независимо или совместно друг с другом.</p>\r\n<p>Химиотерапия – это уничтожение раковых клеток специальными препаратами. Интерканальная терапия осуществляется через поясничный прокол и обеспечивает поступление лекарства непосредственно в спинномозговую жидкость, где может скапливаться большое количество пораженных лейкоцитов.</p>\r\n<p>В случае необходимости, после химиотерапии проводится трансплантация костного мозга. Новые здоровые стволовые клетки нужны для восстановления нормального состояния иммунной системы и крови.</p>",
            "prevention": "",
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